Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C4024702
Disease: Reduced factor X activity
Reduced factor X activity 		3 0 2 0.33 0 0
CUI: C4024722
Disease: Reduced factor VII activity
Reduced factor VII activity 		4 0 2 0.29 0 0
CUI: C0750384
Disease: Coumarin Resistance
Coumarin Resistance 		6 0 2 0.22 0 0
CUI: C1848534
Disease: VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1
VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1 		6 0 2 0.22 0 0
CUI: C0342844
Disease: Disorder of glycoprotein metabolism
Disorder of glycoprotein metabolism 		1 0 1 0.20 0 0
CUI: C1096488
Disease: Hereditary factor IX deficiency disease without inhibitor
Hereditary factor IX deficiency disease without inhibitor 		1 0 1 0.20 0 0
CUI: C1835813
Disease: Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency
Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency 		1 0 1 0.20 0 0
CUI: C1843832
Disease: VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2
VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2 		1 0 1 0.20 0 0
CUI: C2718087
Disease: Vitamin K Deficiency Bleeding
Vitamin K Deficiency Bleeding 		1 0 1 0.20 0 0
CUI: C2749016
Disease: Thrombophilia, X-Linked, Due To Factor Ix Defect
Thrombophilia, X-Linked, Due To Factor Ix Defect 		1 0 1 0.20 0 0
CUI: C2931008
Disease: Congenital disorder of glycosylation type 2A
Congenital disorder of glycosylation type 2A 		1 0 1 0.20 0 0
CUI: C4021060
Disease: Hyperplastic labia majora
Hyperplastic labia majora 		1 0 1 0.20 0 0
CUI: C4022872
Disease: Reduced thyroxin-binding globulin
Reduced thyroxin-binding globulin 		1 0 1 0.20 0 0
CUI: C4280709
Disease: Impaired neutrophil chemotaxis
Impaired neutrophil chemotaxis 		1 0 1 0.20 0 0
CUI: C4317093
Disease: Reduced factor XI activity
Reduced factor XI activity 		7 0 2 0.20 0 0
CUI: C4531146
Disease: Impaired antigen-specific response
Impaired antigen-specific response 		1 0 1 0.20 0 0
CUI: C1859339
Disease: Midfrontal capillary hemangioma
Midfrontal capillary hemangioma 		2 0 1 0.17 0 0
CUI: C2675747
Disease: Coumarin Sensitivity
Coumarin Sensitivity 		2 0 1 0.17 0 0
CUI: C3494186
Disease: Autosomal Hemophilia A
Autosomal Hemophilia A 		2 0 1 0.17 0 0
CUI: C4280698
Disease: Reduced prothrombin antigen
Reduced prothrombin antigen 		2 0 1 0.17 0 0
CUI: C0240671
Disease: Partial thromboplastin time increased (finding)
Partial thromboplastin time increased (finding) 		18 0 3 0.15 0 0
CUI: C0342143
Disease: Hyperthyroidism secondary to amiodarone
Hyperthyroidism secondary to amiodarone 		3 0 1 0.14 0 0
CUI: C1832736
Disease: CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id 		3 0 1 0.14 0 0
CUI: C3151409
Disease: GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE III
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE III 		3 0 1 0.14 0 0
CUI: C3888513
Disease: CYP2C9 polymorphism
CYP2C9 polymorphism 		3 0 1 0.14 0 0